Alpha-tocopherol transfer protein

Alpha-tocopherol transfer protein is a protein that in humans is encoded by the TTPA gene.[5][6][7]

TTPA
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesTTPA, ATTP, AVED, TTP1, alphaTTP, tocopherol (alpha) transfer protein, alpha tocopherol transfer protein
External IDsOMIM: 600415 MGI: 1354168 HomoloGene: 37295 GeneCards: TTPA
Gene location (Human)
Chr.Chromosome 8 (human)[1]
Band8q12.3Start63,048,553 bp[1]
End63,086,053 bp[1]
RNA expression pattern
More reference expression data
Orthologs
SpeciesHumanMouse
Entrez

7274

50500

Ensembl

ENSG00000137561

ENSMUSG00000073988

UniProt

P49638

Q8BWP5

RefSeq (mRNA)

NM_000370

NM_015767
NM_001317723

RefSeq (protein)

NP_000361

NP_001304652
NP_056582

Location (UCSC)Chr 8: 63.05 – 63.09 MbChr 4: 20.01 – 20.03 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

See also

References

  1. GRCh38: Ensembl release 89: ENSG00000137561 - Ensembl, May 2017
  2. GRCm38: Ensembl release 89: ENSMUSG00000073988 - Ensembl, May 2017
  3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. Ouahchi K, Arita M, Kayden H, Hentati F, Ben Hamida M, Sokol R, Arai H, Inoue K, Mandel JL, Koenig M (1995). "Ataxia with isolated vitamin E deficiency is caused by mutations in the alpha-tocopherol transfer protein". Nat Genet. 9 (2): 141–145. doi:10.1038/ng0295-141. PMID 7719340.
  6. Arita M, Sato Y, Miyata A, Tanabe T, Takahashi E, Kayden HJ, Arai H, Inoue K (1995). "Human alpha-tocopherol transfer protein: cDNA cloning, expression and chromosomal localization". Biochem J. 306 (2): 437–443. doi:10.1042/bj3060437. PMC 1136538. PMID 7887897.
  7. "Entrez Gene: TTPA tocopherol (alpha) transfer protein (ataxia (Friedreich-like) with vitamin E deficiency)".

Further reading


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